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rs796053136

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053136(C;G)
Make rs796053136(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165374771
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053136
ebirs796053136
HLIrs796053136
Exacrs796053136
Varsomers796053136
Maprs796053136
PheGenIrs796053136
hapmaprs796053136
1000 genomesrs796053136
hgdprs796053136
ensemblrs796053136
gopubmedrs796053136
geneviewrs796053136
scholarrs796053136
googlers796053136
pharmgkbrs796053136
gwascentralrs796053136
openSNPrs796053136
23andMers796053136
23andMe allrs796053136
SNP Nexus

SNPshotrs796053136
SNPdbers796053136
MSV3drs796053136
GWAS Ctlgrs796053136
Max Magnitude0
ClinVar
Risk rs796053136(G;G)
Alt rs796053136(G;G)
Reference rs796053136(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231281C>G
CLNSRC
CLNACC RCV000189149.2,